Open AccessCCN1 stimulated the osteoblasts via PTEN/AKT/GSK3 β /cyclinD1 signal pathway in Myeloma Bone Disease
Author(s) -
Yan Siyang,
Liu Hui,
Liu Zhaoyun,
Peng Fengping,
Jiang Fengjuan,
Li Lijuan,
Fu Rong
Publication year - 2020
Publication title -
cancer medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.403
H-Index - 53
ISSN - 2045-7634
DOI - 10.1002/cam4.2608
Subject(s) - pten , protein kinase b , western blot , cancer research , pi3k/akt/mtor pathway , chemistry , signal transduction , osteoblast , downregulation and upregulation , microbiology and biotechnology , in vitro , medicine , biology , biochemistry , gene
Backgrounds Myeloma‐related bone disease (MBD) is a common complication of multiple myeloma (MM), which can both decrease life quality and influence the prognosis of the patients. We have found that CCN1 stimulated proliferation and differentiation of osteoblasts in MM in vitro and in vivo, while its mechanism still remains unknown. Method Bone marrow mononuclear cells were collected from MM patients and differentiated into the osteoblasts. After co‐culture with CCN1 in vitro, the intracellular signaling antibody array and western blot were performed to explore the signaling pathway. Furthermore, GSK3 β inhibitor TWS119 was used to check the pathway of CCN1 might have on osteoblasts in vitro. Results For the protein array kit, the expressions of GSK3 β , 4E‐BP1, and PTEN are decreased in CCN1 group. For western blots, the CCN1 group also has lower expression comparing to the control group in PTEN ( P = .031). Meanwhile p‐AKT and cyclinD1 levels have increased in the CCN1 group ( P = .002, P = .039). After adding TWS119 as another group, western blot was performed again to verify the pathway. For upstream proteins PTEN and p‐AKT, TWS119 group has higher expression level compared to that in CCN1 group ( P = .003, P = .001). And for downstream protein cyclinD1, TWS119 group also presented higher level than the control group ( P = .02). CCN1 could have almost the same effect on GSK3 β as the specific inhibitor TWS119 had. Conclusions CCN1 can stimulate osteoblasts through PTEN/AKT/GSK3 β /cyclinD1 pathway in MBD, which has the potential to be a novel therapy of MBD.